Table 1.

Patient characteristics




All patients

Patients with early interim PET

Patients with no early interim PET
No.   99   77   22  
Age, y    
   Mean   40.5   40.1   42.0  
   Median   36.2   36.2   39.4  
   Range   18.6-79.2   18.6-74.0   19.0-79.2  
Follow-up, mo    
   Mean   22,7   23.4   20.1  
   Median   20.8   22.8   18.7  
   Range   2.0-40.8   6.1-40.8   2.0-38.5  
2-year PFS, %   80.2   80.7   78.3  
Sex (%)    
   Male   61 (62)   49 (64)   12 (55)  
   Female   38 (38)   28 (36)   10 (46)  
Clinical stage (%)    
   I   22 (22)   15 (20)   7 (32)  
   II   42 (42)   33 (43)   9 (41)  
   III   27 (27)   23 (30)   4 (18)  
   IV   8 (8)   6 (8)   2 (9)  
No. of regions    
   Mean   3.10   3.22   2.68  
   Median   3   3   2.5  
   Range   1-10   1-10   1-6  
Extranodal disease (%)    
   Yes   18 (18)   14 (18)   4 (18)  
   No   81 (82)   63 (82)   18 (82)  
B symptoms (%)    
   Yes   52 (53)   40 (52)   12 (55)  
   No   47 (48)   37 (48)   10 (46)  
Bulky disease (%)    
   Yes   31 (31)   26 (34)   5 (23)  
   No   68 (69)   51 (66)   17 (77)  
Histologic type (%)    
   NS   61 (62)   51 (66)   10 (46)  
   MC   20 (20)   17 (22)   3 (14)  
   CHL, NOS   8 (8)   3 (4)   5 (23)  
   NLP   10 (10)   6 (8)   4 (18)  
IPS, 1-7    
   Mean   2.77   2.82   2.59  
   Median   3   3   2.5  
   Range   1-6   1-5   1-6  
First-line treatment (%)    
   ABVD   85 (86)   70 (91)   15 (68)  
   ABV/MOPP   3 (3)   2 (3)   1 (5)  
   ABVD/COPP   2 (2)   2 (3)   0 (0)  
   BEACOPP esc.   2 (2)   2 (3)   0 (0)  
   PVAG   2 (2)   1 (1)   1 (5)  
   Radiotherapy only   5 (5)   0 (0)   5 (23)  
Clinical outcome (%)    
   Progression   18 (18)   14 (18)   4 (18)  
   Death
 
5 (5)
 
2 (3)
 
3 (14)
 



All patients

Patients with early interim PET

Patients with no early interim PET
No.   99   77   22  
Age, y    
   Mean   40.5   40.1   42.0  
   Median   36.2   36.2   39.4  
   Range   18.6-79.2   18.6-74.0   19.0-79.2  
Follow-up, mo    
   Mean   22,7   23.4   20.1  
   Median   20.8   22.8   18.7  
   Range   2.0-40.8   6.1-40.8   2.0-38.5  
2-year PFS, %   80.2   80.7   78.3  
Sex (%)    
   Male   61 (62)   49 (64)   12 (55)  
   Female   38 (38)   28 (36)   10 (46)  
Clinical stage (%)    
   I   22 (22)   15 (20)   7 (32)  
   II   42 (42)   33 (43)   9 (41)  
   III   27 (27)   23 (30)   4 (18)  
   IV   8 (8)   6 (8)   2 (9)  
No. of regions    
   Mean   3.10   3.22   2.68  
   Median   3   3   2.5  
   Range   1-10   1-10   1-6  
Extranodal disease (%)    
   Yes   18 (18)   14 (18)   4 (18)  
   No   81 (82)   63 (82)   18 (82)  
B symptoms (%)    
   Yes   52 (53)   40 (52)   12 (55)  
   No   47 (48)   37 (48)   10 (46)  
Bulky disease (%)    
   Yes   31 (31)   26 (34)   5 (23)  
   No   68 (69)   51 (66)   17 (77)  
Histologic type (%)    
   NS   61 (62)   51 (66)   10 (46)  
   MC   20 (20)   17 (22)   3 (14)  
   CHL, NOS   8 (8)   3 (4)   5 (23)  
   NLP   10 (10)   6 (8)   4 (18)  
IPS, 1-7    
   Mean   2.77   2.82   2.59  
   Median   3   3   2.5  
   Range   1-6   1-5   1-6  
First-line treatment (%)    
   ABVD   85 (86)   70 (91)   15 (68)  
   ABV/MOPP   3 (3)   2 (3)   1 (5)  
   ABVD/COPP   2 (2)   2 (3)   0 (0)  
   BEACOPP esc.   2 (2)   2 (3)   0 (0)  
   PVAG   2 (2)   1 (1)   1 (5)  
   Radiotherapy only   5 (5)   0 (0)   5 (23)  
Clinical outcome (%)    
   Progression   18 (18)   14 (18)   4 (18)  
   Death
 
5 (5)
 
2 (3)
 
3 (14)
 

PFS indicates progression-free survival; NS, nodular sclerosis; MC, mixed cellularity; CHL, classic Hodgkin lymphoma; NOS, not otherwise specified; NLP, nodular lymphocyte predominance; ABVD, adriamycin, bleomycin, vinblastine, dacarbazine; ABV/MOPP, adriamycin, bleomycin, vinblastine, mechlorethamine, vincristine, procarbazine, prednisone; ABVD/COPP, cyclophosphamide, vincristine, procarbazine, prednisone; BEACOPP, bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, prednisone; and PVAG, prednisone, vinblastine, doxorubicin, gemcitabine.

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